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Monique Hooley

I am investigating whether normal astrocytic functions are altered in Alzheimer’s Disease (AD).

Monique Hooley

PhD Student - Hardingham & Spires-Jones Groups

  • 1 George Square
  • Edinburgh
  • EH8 9XD

Contact details

Personal profile

  • Wellcome Trust 4 Year Translational Neuroscience PhD student (2016-present)
  • Pharmacology Msci, University of Bristol (2012-2016)
  • Industrial placement at Pfizer (2014-2015)

Research

Astrocytes are the most abundant cell type in the brain. They are involved in a number of functions, including providing nutrients to nervous tissue and regulating extracellular ion balance. I am investigating whether normal astrocytic functions are altered in Alzheimer’s Disease (AD). I am utilising in vitro and in vivo models of AD to conduct unbiased searches for alterations in astrocytic gene expression in the context of synapse loss. I will compare these results to those found in human AD cases to assess the suitability of these models. 

 

 

Figure 1. Primary mouse astrocyte DIV14. Glutamate transporters EAAT1 (green) and EAAT2 (red).
Figure 1. Primary mouse astrocyte DIV14. Glutamate transporters EAAT1 (green) and EAAT2 (red).

 

Figure 2. Hippocampal tissue from a mouse model of AD. Showing presynaptic protein synaptophysin (green) apposing postsynaptic P
Figure 2. Hippocampal tissue from a mouse model of AD. Showing presynaptic protein synaptophysin (green) apposing postsynaptic PSD-95 (red) and a small plaque (white). Tissue processed by array tomography. Figure 2. Hippocampal tissue from a mouse model of AD. Showing presynaptic protein synaptophysin (green) apposing postsynaptic PSD-95 (red) and a small plaque (white). Tissue processed by array tomography.
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